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Vol. 273, Issue 3, 1380-1386, January 16, 1998
From the Institute of Clinical Pharmacology, Charite-Humboldt
University of Berlin, 10098 Berlin/Max Delbrueck Centrum for Molecular
Medicine, 13125 Berlin-Buch, Germany, the Phosphatidylcholines (PCs) with branched fatty
acyl chains substituted in the two positions of the main chains
(branched PCs) have been shown to be potent activators of the side
chain cleavage activity of cytochrome P450SCC (CYP11A1) (Schwarz, D.,
Kisselev, P., Wessel, R., Jueptner, O., and Schmid, R. D. (1996)
J. Biol. Chem. 271, 12840-12846). The present study
reports on the effect of a series of branched PC on cholesterol
binding, membrane integration, and protein exchange in large
unilamellar vesicles prepared by an extrusion technique. Enzyme
kinetics using vesicles as well as optical titration using a micelle
system with the detergent Tween 20 demonstrate that activation is
correlated with the fraction of P450SCC in the high spin form. The
potency of branched PCs both to activate the enzyme and to induce spin
state changes increases with increasing lengths of both the branched
and main fatty acyl chains. We found that the extent as well as the
rate of integration of P450SCC into vesicle membranes studied by gel
chromatography and stopped flow kinetics were increased by branched PC.
Finally, it is demonstrated by measurement of the enzymatic activity in primary and secondary vesicles that branched PCs are potent in retaining a very rapid exchange of P450SCC between vesicles, in contrast to cardiolipin, that partially inhibits this exchange process.
The data suggest that different properties of P450SCC in membrane
systems including cholesterol binding, membrane integration, and
protein exchange are affected by branched PCs and probably by other
phospholipids, too, and therefore must be considered in an explanation
of the observed high stimulation of activity.
Branched Phosphatidylcholines Stimulate Activity of Cytochrome
P450SCC (CYP11A1) in Phospholipid Vesicles by Enhancing Cholesterol
Binding, Membrane Incorporation, and Protein Exchange
,
Institute of
Bioorganic Chemistry, Academy of Sciences of Belarus, 220141 Minsk,
Belarus, and the § Institute for Technical Biochemistry,
University Stuttgart, 70569 Stuttgart, Germany
Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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